Canonical Allele Identifier: CA396537159

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211703C>G , CM000678.2:g.79211703C>G	GRCh38
NC_000016.9:g.79245600C>G , CM000678.1:g.79245600C>G	GRCh37
NC_000016.8:g.77803101C>G	NCBI36
NG_011698.1:g.1117050C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.1152C>G (WWOX) MANE Select	NP_057457.1:p.Pro384=
ENST00000566780.6:c.1152C>G (WWOX) MANE Select	ENSP00000457230.1:p.Pro384=
NM_001291997.1:c.813C>G (WWOX)	NP_001278926.1:p.Pro271=
NM_001291997.2:c.813C>G (WWOX)	NP_001278926.1:p.Pro271=
NM_016373.3:c.1152C>G (WWOX)	NP_057457.1:p.Pro384=
ENST00000402655.6:c.505C>G (WWOX)	ENSP00000384238.2:p.Leu169Val
ENST00000406884.6:c.612C>G (WWOX)	ENSP00000384495.2:p.Pro204=
ENST00000539474.6:c.581C>G (WWOX)	ENSP00000445210.2:p.Pro194Arg
ENST00000566103.1:n.219C>G (WWOX)
ENST00000566780.5:c.1152C>G (WWOX)	ENSP00000457230.1:p.Pro384=
ENST00000569332.5:c.*949C>G (WWOX)	ENSP00000454788.1:n.*949C>G
ENST00000683929.1:c.*266C>G (WWOX)	ENSP00000507689.1:n.*266C>G
XM_011523100.1:c.1248C>G (WWOX)	XP_011521402.1:p.Pro416=
XM_011523103.3:c.*124C>G (WWOX)	XP_011521405.1:n.*124C>G
XM_017023279.1:c.238C>G (WWOX)	XP_016878768.1:p.Leu80Val
XM_024450279.1:c.*1227G>C (MAF)	XP_024306047.1:n.*1227G>C
XR_001751902.2:n.4429G>C (MAF)
XR_002957802.1:n.4429G>C (MAF)
XR_002957803.1:n.4429G>C (MAF)
XR_002957804.1:n.4429G>C (MAF)